A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528161



Internal ID15455454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42574295..42669053hg38UCSC Ensembl
Innerchr20:41202935..41297693hg19UCSC Ensembl
Innerchr20:40636349..40731107hg18UCSC Ensembl
Innerchr20:40636349..40731107hg17UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3894759
hg1994759
hg1894759
hg1794759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv247n21
Supporting Variantsnssv704710
Samples
Known GenesPTPRT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528161
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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